What Can MR Signal Tell Us About the Spin Environment?

\(T_1\) and \(T_2\) Relaxation Times

Example Real-World Application Magnetic Resonance Imaging (MRI) can provide lots of diagnostic information in medicine because of the many different contrast mechanisms available. The most common ways of providing contrast to differentiate between different types of tissues involve \(T_1\)- and \(T_2\)-weighted images. (1)

Expected Learning Outcomes

At the end of this module, students should be able to…

  1. Differentiate \(T_1\) and \(T_2\) relaxation mechanisms for signal decay (Scientific Ability B9)

  2. Design an application experiment that can determine which sample has longest \(T_1\) (Scientific Ability D2)

  3. Choose correct experimental parameters to optimize \(T_1\) contrast for different samples (Scientific Ability A4)

“The direct knowledge of matter that mankind can acquire is a knowledge of the average behaviour and relations of the crowd of molecules.”

Background Information

relaxation - the process of a system returning (‘relaxing’) back to its stable equilibrium state

We have seen that we can control quantum spins by using electromagnetic pulses that can resonate at the spins’ Larmor frequency for a given magnetic field strength. In this module, we explore the other information can be gleamed from magnetic resonance signal. In particular, looking at how quickly the signal decays away in a process called relaxation can tell us a lot about the local magnetic environment of our quantum spins.

time constant - the time it takes for an exponential decay to reach \(e^{-1} \approx 0.37\) (or 37%) of its initial amplitude

Two primary sources of relaxation are characterized by two different times, \(T_1\) and \(T_2\). These times are related to time constants one would see in exponential decays of the form \(e^{-t/T}\). The larger the time constant \(T\), the longer it takes for the signal to decay.

In this module, you will explore the different mechanisms that cause \(T_1\) and \(T_2\) relaxation, as well as determine how we can design experiments that can make use of these relaxation mechanisms to better characterize our samples.

Classwide Discussion

  1. All the protons see the exact same local magnetic environment
  1. All the protons see slightly different local magnetic environments

Explain your choice. Hint: consider what you would want all the protons to be doing in order to maximize the MR signal.

Observation Experiment: \(T_2\) Relaxation

Image source (2)

Felix Bloch - a Physics Nobel Prize winner with Edward Mills Purcell in 1952 for independently developing new ways and methods for nuclear magnetic precision measurements - techniques that would blossom into the field of NMR. When Hitler ascending to power in 1933, Bloch left Germany and came to the United States, where he completed his Nobel-prize-winning work.

“Free imagination is the inestimable prerogative of youth and it must be cherished and guarded as a treasure.” - Felix Bloch, Nobel Prize Banquet Speech

In order to uncover the different mechanisms that cause relaxation, let’s return to the Bloch Simulator which conveniently has some \(T_1\) and \(T_2\) control knobs. Let’s see how changing these knobs affects our quantum spins and the measured MR signal.

Guided Inquiry Questions

  1. First let’s initialize our spin-state and then knock the spins down into the x-y plane using a hard-\(90^\circ\) pulse. Is there any MR signal decay? Explain how you come to your conclusion.

  2. In the upper-left menu, click on ‘Relaxation: Off’ and you can see that both ‘T1’ and ‘T2’ are set to infinity. Why is having both ‘T1’ and ‘T2’ set to infinity the same as having the relaxation turned ‘off’?

  3. Now change the ‘T2’ value to some finite value (while leaving ‘T1’ at infinity). Describe what happens to the net nuclear magnetization vector, \(\vec{M}\) and sketch the resulting plot of \(|M_{xy}|\) and \(M_x\).

  4. Describe how \(T_2\) relaxation appears to cause the MR signal to decay.

\(T_2\) Relaxation

The \(T_2\) relaxation process is primarily due to magnetic interactions between quantum spins and is sometimes instead called spin-spin relaxation. We saw examples of this relaxation process in the free induction decay, characterized by the time constant \(T_2^*\). Where \(T_2^*\) is primarily caused by external magnetic field inhomogeneities, \(T_2\) is primarily caused by local magnetic field differences for the quantum spins. Even if we apply the most ideal, homogeneous magnetic field, we still expect some signal decay because of the quantum spins interacting with the local magnetic field caused by nearby quantum spins, and this inherent decay is characterized by \(T_2\) and tells us something explicitly about the local magnetic environment being felt by the spins - namely, if all spins are seeing identical magnetic environments or not.

Similar to \(T_2^*\), the spin-spin interactions causes the spins to dephase from each other, causing \(|M_{xy}|\) to get smaller and smaller as the spins get farther and farther ‘out of step’ with each other. Since this dephasing happens in the transverse (xy) plane, \(T_2\) relaxation is also sometimes called transverse relaxation.

\(T_2\) Relaxation

  • Spin-spin relaxation or transverse relaxation
  • Decay of transverse magnetization, \(M_{xy}\) (represented by green arrow in figure)
  • Primarily caused by local magnetic field differences

Guided Inquiry Questions

  1. Given the description of what causes \(T_2^*\) relaxation versus \(T_2\) relaxation, which do you think is always the larger value, \(T_2\) or \(T_2^*\)? Why?

  2. Below is some FID data acquired from a mineral oil sample in a 0.5-T field. What is the approximate \(T_2^*\) value for this sample? Hint: you want to find the time when the signal reaches 37% of its initial amplitude.

  1. If Sample A has a much longer \(T_2\) time than Sample B, what can you say about the local magnetic environments of Sample A in comparison to Sample B?

Observation Experiment: \(T_1\) Relaxation

Let’s return to the Bloch Simulator to explore the effects of \(T_1\) relaxation on the spins in the Bloch sphere representation and how this causes relaxation.

Guided Inquiry Questions

  1. Turn off relaxation (by setting ‘T1’ and ‘T2’ both to infinity), initialize the spin-state, and then knock the spins down into the x-y plane using a hard-\(90^\circ\) pulse. Now change ‘T1’ to some finite value. Observe, sketch, and describe what happens.

  2. You may have noticed that it is impossible to set ‘T2’ larger than ‘T1’. This is not a bug in the simulator but turns out to be a physical fact: \(T_2 \leq T_1\). That means it may be difficult to fully disentangle the two from each other, but thinking about the difference of the spin dynamics compared with the \(T_2\) relaxation observed above, how does \(T_1\) relaxation contribute to the decaying MR signal?

  3. If \(T_2\) relaxation is also called transverse (xy) relaxation, what might be a good name for \(T_1\) relaxation?

\(T_1\) Relaxation

The \(T_1\) relaxation process is primarily due to quantum spins exchanging energy with it’s environment in order to return to it’s energetically stable equilibrium state (the \(\alpha\) state, aligned with the magnetic field along the z-axis). This relaxation process is sometimes instead called spin-lattice relaxation (referring to the crystal lattice structure of many solid materials). We know that nature prefers to return to its equilibrium state, and \(T_1\) is the time that characterizes how fast quantum spins will naturally return to equilibrium. Many factors determine the \(T_1\) time for a sample, most notably the strength of the magnetic field (which determines how much energy is needed to be transferred to transition to the lowest energy state) and the temperature of the sample (which determines how much energy the lattice can potentially exchange with the spin).

The effect of \(T_1\) is best viewed by plotting \(M_z\) after a pulse has been applied to the spins and watching how fast the signal returns to equilibrium. This follows an exponential recovery curve \((1-e^{-t/T})\) and longer \(T_1\) times leads to a longer recovery. Since \(T_1\) relaxation is mostly due to the quantum spins realigning with the external magnetic field along the z-axis, \(T_1\) relaxation is also sometimes called longitudinal relaxation because the signal is recovering along the magnetic field direction.

Fig. 22 from MRI Made Easy by Prof. Dr. Hans H. Schild (3). Coupling of a \(T_1\)- and a \(T_2\)-curve resembles a mountain with a slope. It takes longer to climb a mountain than to slide or jump down, which helps to remember that \(T_1\) is normally longer than \(T_2\).

\(T_1\) Relaxation

  • Spin-lattice relaxation or longitudinal relaxation
  • Decay of longitudinal magnetization, \(M_{z}\)
  • Primarily caused by exchanging energy with local environment

Pannini, CC BY-SA 3.0 https://creativecommons.org/licenses/by-sa/3.0, via Wikimedia Commons. You can find more information on the file information page.

Guided Inquiry Questions

  1. Given the description of what causes \(T_1\) relaxation versus \(T_2\) relaxation, why do you think the \(T_1\) time is always longer than \(T_2\)?

  2. Describe the magnetic environment that would be necessary for \(T_2\) to be equal to \(T_1\).

Feel free to talk through potential options with the instructor!

  1. We can only acquire signal along the transverse (xy) plane, but \(T_1\) is most easily determined from plotting \(M_z\) at different time points. How might we acquire the \(M_z\) information? Hint: the first point of an FID experiment is essentially the \(M_z\) value right before the hard-\(90^\circ\) pulse.

Application Experiment: Which sample has the longest \(T_1\)?

pulse sequence - the time sequence of electromagnetic pulses applied to a sample and the time periods where MR signal is acquired Fun fact! Due to the sensitivity of the NMR spectrometer receiver, MR signal is never acquired during the transmission of RF pulses. These pulses are typically high-power and would easily overwhelm the detector. Spectrometers that use the same coil for both transmission and receiving have electronics that are very cleverly designed to ensure the that the RF pulses (and even the reflections of the pulses) do not make it to the receiver to potentially damage the electronic detection system. If scientists want to view the pulses themselves, they use another detection system (usually simply a small ‘pick-up’ coil attached to an oscilloscope).

The goal for this activity is for you to develop an experimental procedure to be able to determine which of two samples has the longer \(T_1\) time. MR experimental procedures are demonstrated by a pulse sequence which shows the timing of application of different pulses and when signal will be acquired. For example, the pulse sequence for the free induction decay experiment is shown below.

Along with the pulse sequence to provide the timing for transmitting pulses and acquiring signal, MR experimental procedures also include the repetition time (TR) used because most experiments are repeated multiple times so the signal can be averaged together to improve signal-to-noise.

Guided Inquiry Questions

  1. Describe an experimental procedure you can use to compare the \(T_1\) times of two samples. Include a pulse sequence for your experiment/s.

  2. Why is it important to consider the repetition times (TR) are you going to use if you run multiple experiments?

Once you are happy with your experimental procedure, perform your experiment with the provided samples and use your datat to determine which sample has the longer \(T_1\) time.

Reflection Questions

  1. What will happen to your MR signal if you choose a repetition time (TR) that is much shorter than the \(T_1\) time for your sample?

  2. Will using too short of a TR time impact the measured \(T_2\) time?

Below is a plot of the \(T_1\) curves for brain tissue compared with cerebrospinal fluid (CSF). You should use this plot to answer the following questions.

Fig. 32 from MRI Made Easy by Prof. Dr. Hans H. Schild (3).

  1. Which has the longer \(T_1\) time, brain tissue or cerebrospinal fluid?

  2. You are designing a \(T_1\)-weighted MRI pulse sequence that needs to highlight brain tissue from the surrounding cerebrospinal fluid. Looking at the \(T_1\) curves provided, which of the TR times (TR\(_\text{short}\) or TR\(_\text{long}\)) would be a better choice? Why?